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Symbol Name ID |
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| Synonyms | 3PGDH, 3-PGDH, A10, PGAD, PGD, PGDH, SERA | ||||||||||||||||||
| Feature Type | protein coding gene | ||||||||||||||||||
| Genetic Map | |||||||||||||||||||
| Sequence Map |
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Vertebrate homology |
HomoloGene:39318 Vertebrate Homology Class 1 human; 1 mouse; 1 rat; 1 chimpanzee; 1 rhesus macaque; 1 cattle; 3 dog; 1 chicken; 1 zebrafish Protein SuperFamily: D-3-phosphoglycerate dehydrogenase with ACT domain Gene Tree: Phgdh |
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| Human homologs |
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Alleles and phenotypes |
All alleles(5) :
Targeted(4)
Gene trapped(1)
Mice homozygous for a null allele die by E13.5 and exhibit abnormal neural development. Phenotype Images(2) |
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Gene Ontology (GO) classifications |
All GO classifications: (25 annotations)
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| Expression |
Literature Summary: (5 records) Data Summary: Results (94) Tissues (94) Images (11) Theiler Stages: 22
External Resources: Allen Institute GEO ArrayExpress |
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Molecular reagents |
All nucleic(11)
cDNA(10)
Primer pair(1)
Microarray probesets(5) |
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Other database links |
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| Sequences |
All sequences(45) RefSeq(2) UniProt(2) |
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| Polymorphisms | SNPs(208 from dbSNP Build 128) | ||||||||||||||||||
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Protein-related information |
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| References |
(Earliest) J:11875
Miller IJ, et al., A novel, erythroid cell-specific murine transcription factor that binds to the CACCC element and is related to the Kruppel family of nuclear proteins. Mol Cell Biol. 1993 May;13(5):2776-86 (Latest) J:184368 Mukhopadhyay P, et al., Strain-specific modifier genes governing craniofacial phenotypes. Birth Defects Res A Clin Mol Teratol. 2012 Mar;94(3):162-75 All references(38) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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